Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_provenance.
- NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_assertion description "[This finding and the previous findings of a 45% frequency of phenotypic color vision defects in patients with AMN may suggest that the ALD/AMN gene lies 5' to the red pigment gene and that the frequent phenotypic color vision anomalies owe their origin to deleted DNA that includes regulatory genes for color vision.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_provenance.
- NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_assertion evidence source_evidence_literature NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_provenance.
- NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_assertion SIO_000772 2309698 NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_provenance.
- NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_assertion wasDerivedFrom befree-20140225 NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_provenance.
- NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_assertion wasGeneratedBy ECO_0000203 NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP907703.RAto0IJOf2bx0DKz6AldgzMAFAl2IHjsH4Zwg83H_ngiU130_provenance.